Literature DB >> 20306757

Boom in clinical research industry: a dangerous trend.

Vikas Bajpai1, Anoop Saraya.   

Abstract

Over the last decade or so India has witnessed a phenomenal growth in the clinical trial industry. The projections forecast a continuing growth of this trend. It has been predicted that by 2011 India will be in charge of 15% of global clinical trials. The enthusiasm for the growth of this industry in India is shared not just by the major pharmaceutical companies and CROs but also equally so by government agencies. The raison d'être for medical research is that it should lead to maximum possible benefit to the largest number of people. Hence, an examination of the extent to which public good is served can act as a measure for objective analysis of this exponential increase in the clinical trial industry. After all it is the health and lives of the people that are at stake. On the face of it, it would seem that all trials testing the safety and efficacy of various molecules, by their very nature work towards public welfare as they are indispensible to the development of any drug including the life-saving ones. An increasing number of clinical trials at all stages in a product's life cycle are funded by the pharmaceutical industry. It would then seem that the industry-sponsored medical research is necessarily furthering the larger objective of human wellbeing. However, the operations of the pharmaceutical industry, the nature of the processes involved and the operative motives are a bit too complex to facilitate this larger objective so simply, just as yet. This warrants a closer look at the various aspects of industry-sponsored clinical research.

Entities:  

Mesh:

Year:  2009        PMID: 20306757

Source DB:  PubMed          Journal:  Trop Gastroenterol        ISSN: 0250-636X


  3 in total

1.  Clinical Trials Registry - India: A decadal perspective.

Authors:  Mendu Vishnu Vardhana Rao; Mohua Maulik; Atul Juneja; Tulsi Adhikari; Saurabh Sharma; Jyotsna Gupta; Yashmin Panchal; Neha Yadav
Journal:  Indian J Pharmacol       Date:  2020 Jul-Aug       Impact factor: 1.200

2.  Comparative effect sizes in randomised trials from less developed and more developed countries: meta-epidemiological assessment.

Authors:  Orestis A Panagiotou; Despina G Contopoulos-Ioannidis; John P A Ioannidis
Journal:  BMJ       Date:  2013-02-12

3.  Comparison of good clinical practice compliance and readability ease of the informed consents between observational and interventional clinical studies in the Emirates.

Authors:  Satish Chandrasekhar Nair; Halah Ibrahim; Omar Sherif Askar
Journal:  Perspect Clin Res       Date:  2016 Jul-Sep
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.